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Submit ReviewInactive isomer of GSK J4; also cell permeable ester derivative of the inactive control, GSK J2.
Active Analog also available.
This compound is supplied in conjunction with the Structural Genomics Consortium. For further characterization details of GSK J5, a cell permeable inactive isomer of GSK J1, please visit the GSK J1 probe summary on the SGC website.
分子量 | 417.5 |
公式 | C24H27N5O2 |
储存 | Store at RT |
纯度 | ≥98% (HPLC) |
CAS Number | 1394854-51-3 |
PubChem ID | 78243729 |
InChI Key | LQPGVGSKBNXQDU-UHFFFAOYSA-N |
Smiles | O=C(CCNC1=NC(C2=CC=CN=C2)=NC(N3CCC(C=CC=C4)=C4CC3)=C1)OCC |
上方提供的技术数据仅供参考。批次相关数据请参见分析证书。
Tocris products are intended for laboratory research use only, unless stated otherwise.
参考文献是支持产品生物活性的出版物。
Kruidenier et al (2012) A selective jumonji H3K27 demethylase inhibitor modulates the proinflammatory macrophage response. Nature 488 404 PMID: 22842901
关键词: GSK J5, GSK J5 supplier, GSKJ5, histone, demethylases, inhibitors, inhibits, UTX, JMJD3, KDM6, H3K27, epigenetics, Histone, Demethylases, 4689, Tocris Bioscience
引用文献是使用了 Tocris 产品的出版物。 GSK J5 的部分引用包括:
Bayo et al (2018) Jumonji Inhibitors Overcome Radioresistance in Cancer through Changes in H3K4 Methylation at Double-Strand Breaks. Cell Rep 25 1040 PMID: 30355483
Carey et al (2015) Intracellular α-ketoglutarate maintains the pluripotency of embryonic stem cells. Int J Nanomedicine 518 413 PMID: 25487152
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Tocris offers the following scientific literature in this area to showcase our products. We invite you to request* your copy today!
*请注意,Tocris 仅会向正规科研企业/机构地址发送文献。
Written by Susanne Müller-Knapp and Peter J. Brown, this review gives an overview of the development of chemical probes for epigenetic targets, as well as the impact of these tool compounds being made available to the scientific community. In addition, their biological effects are also discussed. Epigenetic compounds available from Tocris are listed.